View genomic variant #0000003496

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.153640536G>C
Published as -
GERP 4.140
Segregation -
DB-ID TAZ_000141 See all 2 reported entries
MSCV MSCV_0003496
dbSNP ID -
Frequency -
Sources ; BSF_TAZ;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

5 entries on 1 page. Showing entries 1 - 5.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
TAZ 00000321 NM_000116.3 0000003496 ?/? - 2/10 c.223G>C p.(Asp75His) probably_damaging(0.997) missense_variant - deleterious(0)
TAZ 00000323 NM_181311.2 0000003496 ?/? - 2/10 c.223G>C p.(Asp75His) probably_damaging(0.997) missense_variant - deleterious(0)
TAZ 00000322 NM_181312.2 0000003496 ?/? - 2/10 c.223G>C p.(Asp75His) probably_damaging(0.997) missense_variant - deleterious(0)
TAZ 00000324 NM_181313.2 0000003496 ?/? - 2/10 c.223G>C p.(Asp75His) probably_damaging(0.997) missense_variant - deleterious(0)
TAZ 00000320 NR_024048.1 0000003496 ?/? - 2/10 n.527G>C - - non_coding_transcript_exon_variant,non_coding_transcript_variant - -
Legend  


MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None